Is DVL3 p.Glu623Asp (c.1869G>C) pathogenic?

DVL3 p.Glu623Asp (c.1869G>C) is classified Conflicting classifications of pathogenicity in DVL3 (ClinVar, Conflicting submitters, 2 submitters; last evaluated 2026-02-01). AlphaMissense: likely benign (0.1128); Very rare (popmax 0.00702%, nfe); Associated with Inborn genetic diseases.

What condition is associated with DVL3 p.Glu623Asp (c.1869G>C)?

DVL3 p.Glu623Asp (c.1869G>C) is associated with Inborn genetic diseases (ClinVar).

How common is DVL3 p.Glu623Asp (c.1869G>C) in the general population?

DVL3 p.Glu623Asp (c.1869G>C) is very rare (popmax 0.00702%, nfe) (gnomAD).

What do computational predictors say about DVL3 p.Glu623Asp (c.1869G>C)?

AlphaMissense predicts likely benign (score 0.1128) — an in-silico prediction, not a clinical call.

DVL3 p.Glu623Asp

c.1869G>C · rs768998141 · VCV2198982

Conflicting classifications of pathogenicity Conflicting submitters

Classification

Conflicting classifications of pathogenicity

ClinVar

Review

Conflicting submitters ★☆☆☆

ClinVar · 2 submitters

AlphaMissense

likely benign

0.1128 · ACMG-weighted

gnomAD v4.1

Rare

very rare (popmax 0.00702%, nfe)

Missense predictors

0/3 damaging

AlphaMissense, REVEL, SaProt

Conditions

Inborn genetic diseases

Computational evidence

Protein change
AlphaMissense	0.1128	likely benign
REVEL	0.116	moderately benign-leaning
SaProt	LLR -7.29	tolerated
⇒ AlphaMissense, REVEL and SaProt all call this tolerated.
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Constraint at this position
Conservation	phyloP 3.8	GERP 0.3, phastCons 1
Regional constraint	o/e 0.98	unconstrained · MANE · 2,688 bp · p 0.69 · regional, not allelic
Overall
CADD	21.1	PHRED · no single calibrated threshold — expert panels disagree

AlphaMissense carries the ACMG weight for missense; REVEL and SaProt are independent agreement signals.

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.00702% European (non-Finnish) · 82/1,167,816 alleles

Filtering AF 0.00577% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.0053%

Overall 0.00548% 87/1,587,768 alleles · very rare

Ancestry group	Frequency	1 in
European (non-Finnish)grpmax	0.00702%	14,242
Finnishnot grpmax-eligible	0.00651%	15,357
Remaining individualsnot grpmax-eligible	0.00163%	61,338

Rarity supports pathogenicity (ACMG PM2); frequency above a disease-specific BA1/BS1 threshold argues against it. A variant frequent in one ancestry group can be near-absent in others, so a single global figure can mislead.

Variant & gene context

Gene: DVL3
Protein: p.Glu623Asp
Coding: c.1869G>C
MANE Select: NM_004423
dbSNP: rs768998141
Type: single nucleotide variant
Location: chr3:184170473 (GRCh38)
Gene constraint: LOEUF 0.536 · pLI 0.70 (gnomAD)
Structure: AlphaFold pLDDT 59.50 · 9 PDB
Residue 623: the 'disordered' region

Full DVL3 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

Inborn genetic diseases — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

Similar variants

DVL3 p.Ala359Thr Uncertain significance ★★ ⚠ same condition
DVL3 p.Ala565Val Uncertain significance ★★ ⚠ same condition
DVL3 p.Ala593Val Uncertain significance ★★ ⚠ same condition
DVL3 p.Ala629Thr Uncertain significance ★★ ⚠ same condition
DVL3 p.Arg145Gln Uncertain significance ★★ ⚠ same condition
DVL3 p.Arg157Gln Uncertain significance ★★ ⚠ same condition
DVL3 p.Arg166Trp Uncertain significance ★★ ⚠ same condition
DVL3 p.Arg167Gln Uncertain significance ★★ ⚠ same condition

Built on 18 open, versioned datasets — ClinVar, gnomAD, AlphaMissense, REVEL, ClinGen & more — plus Sugi Variant's own cross-source analysis. Source data 2026-01–2026-10, ClinVar 2026-10. Full sources & versions →

Cite Sugi Variant

Gür T. Sugi Variant: A Deterministic Per-Variant Germline Reference from a Knowledge Graph for Humans and AI Agents. 2026. doi:10.5281/zenodo.21509445. This variant: https://sugi.bio/variant/dvl3-p-glu623asp (accessed [today's date]).

Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown